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A Study to Compare ABP 234 and Keytruda® (Pembrolizumab) in Participants With Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer

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NCT06311721 · readout in 509 d

Sponsored by Amgen (industry) · AMGN — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
315actual
Sites
218
Countries
Argentina, Austria, Brazil +20

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-09-09actualWhen the study began enrolling
Primary completion2028-01-10estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-04-24estimatedThe whole study's end, after follow-up
First posted2024-03-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer

Interventions

  • Drug: ABP 234
  • Drug: Pembrolizumab (US) — also filed as Keytruda®
  • Drug: Pembrolizumab (EU) — also filed as Keytruda®

Primary outcomes

what the primary-completion date above is the date OF
Area under the serum concentration-time curve (AUC) from time 0 to 21 days (AUC21d) of ABP 234
measured 21 days
AUC21d of pembrolizumab (US)
measured 21 days
AUC21d of pembrolizumab (EU)
measured 21 days
AUC at steady state between Week 16 and Week 19 (AUCtau_ss) of ABP 234
measured Week 16 through Week 19
AUCtau_ss of pembrolizumab (US)
measured Week 16 through Week 19
AUCtau_ss of pembrolizumab (EU)
measured Week 16 through Week 19

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